Broadening the rare earth ion emission bandwidth, increasing emission cross section, and or shifting peak emission wavelength in nd doped aluminate or silicate glasses

ABSTRACT

The invention relates to a Nd-doped, aluminate-based or silicate-based, laser glass having a peak emission wavelength that is longer than 1059.7 nm, an emission cross section (σ em ) of ≧1.5×10 −20  cm 2 , and/or an emission bandwidth (Δλ eff ) of ≧28 nm, while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T g  and low nonlinear index, n 2 .

SUMMARY OF THE INVENTION

The invention relates to glasses for use in solid laser applications, particularly short-pulse, high peak power laser applications. In particular, the invention relates to glasses for a mixed glass laser system wherein an aluminate or silicate laser glass is used in combination with a phosphate laser glass.

Further, the invention relates to Nd-doped aluminate or silicate glass, suitable for use in a mixed glass laser system, wherein (a) the Nd-doped aluminate or silicate glass has a peak emission at a wavelength above 1060 nm (particularly above 1067 nm for Nd-doped aluminate glass), (b) the Nd-doped aluminate or silicate glass has a broadened emission cross section, and/or (c) the Nd-doped aluminate or silicate glass has a broadened emission bandwidth, while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g), high emission cross section, and low nonlinear index, n₂. In addition, the invention relates to a method of shifting the peak emission wavelength of the emission band width to a longer wavelength, e.g., a wavelength which is above 1060 nm for an Nd-doped silicate glass or above 1067 nm for an Nd-doped aluminate glass, and/or increasing the emission cross section, and/or broadening the emission bandwidth for a Nd-doped aluminate or silicate glass, while again maintaining properties that render the glass suitable for commercial use.

One general trend in solid state lasers is to make high energy lasers with shorter pulse lengths, which drives the power in the pulse to very high numbers. For example, a 10 k Joule laser with a 10 nsec pulse length is a power of 1 TW (1 TW=10000 J/10 nsec). The trend towards the use of high energy lasers with shorter pulse lengths is described in “Terrawatt to pettawatt subpicosecond lasers”, M. D. Perry and G. Mourou, Science, Vol 264, 917-924 (1994).

In high power and short-pulse laser applications, such as the present petawatt laser systems and ultra-short pulsed lasers (lasers producing light pulses with a duration of, for example, one picosecond or less) as well as the future exawatt lasers systems, it is desirable that the solid-sate laser medium have a broad emission bandwidth. See, for example, the Hercules laser described in Laser Focus World, April 2008, pp. 19-20, which uses Ti doped sapphire crystals. An important factor in designing laser systems that utilize short pulses is to find gain materials with broad emission bandwidth for the laser transition.

For mode-locked lasers, it is a well-known result, from Fourier's theorem, that the narrower the pulse width, the larger the gain bandwidth required to generate that pulse; thus transform limited. For an inhomogeneously broadened line width of a laser medium, if the intensity of pulses follows a Gaussian function, then the resulting mode-locked pulse will have a Gaussian shape with the emission bandwidth/pulse duration relationship of: Bandwidth X Pulse Duration ≧0.44. See, W. Koechner, Solid State Laser Engineering, 6 ed, Springer Science, 2005 (pg 540). Clearly, to achieve ever shorter pulse durations it is a requirement to identify glasses with a broad emission bandwidth.

The absorption and emission of photons by an active ion in a gain material is proportional to the absorption and emission cross section, where the cross section represents the gain per unit length per the population inversion density. During laser operation, a high cross-section means that fewer photons are needed to saturate any given transition during pumping and stimulated emission. Thus, a high cross section is advantageous in that it improves the probability of absorption and emission in gain materials leading to higher efficiencies with better tolerance for optical losses.

Titanium-sapphire [Ti:Sapphire, Ti:Al₂O₃] crystals have a broad emission bandwidth as well as high laser cross sections over a broad region of emission. These properties, in combination with the excellent thermal, physical and optical properties of the sapphire crystal, make this a gain material of choice for active solid-state ultra-short pulsed lasers. According to the Füchtbauer-Ladenburg equation, the product of emission cross-section, emission bandwidth and radiative lifetime must be approximately constant for a given emitting ion. Thus, a high cross-section and large emission bandwidth necessitates a short lifetime. The short fluorescence lifetime of Ti:Sapphire requires pumping with other lasers (for example, Ti doped sapphire short pulse lasers are often pumped by Nd-doped glass lasers which in turn are pumped by flashlamps). This adds to the overall architecture and complexity of the laser system, particularly when attempting to scale up to exawatt or high-pettawatt peak powers, Moreover, being a crystalline material, generating large apertures of Ti:Sapphire material with the requisite optical qualities is challenging and expensive.

Another design for short pulsed lasers utilizes rare earth doped glasses. The advantages of such glasses over crystals include lower costs and higher available energies (since glass can be manufactured in large sizes of high optical quality, while Ti doped sapphire is limited in size). In addition, simpler designs can be implemented since the glass gain materials can be directly pumped by flashlamps. Unlike lasers using Ti:Sapphire crystals, the glass approach does not require one to first build pump lasers.

Laser glasses are produced by doping host glass systems with rare earth elements that have the ability to lase, such as neodymium, ytterbium, and erbium. The lasing ability of these rare earth doped laser glasses results from the light amplification achieved by stimulated emission of the excited rare earth element ions within the glass.

Glasses have a proven track record as a host matrix suitable for rare-earth ions that provide the large apertures necessary for high average power laser systems. This is especially true for phosphate glasses which can be manufactured in large quantities and can be made platinum particle free, when manufactured under the right processing conditions.

In addition to phosphate glasses, tellurite, silicates, borates, borosilicates, and aluminates have also been used as host glass matrix systems for lasing ions. Silicate, borate, borosilicates, and aluminate glasses have broader emission bandwidth for Nd lasing ions, in comparison to phosphate glasses.

However, there are disadvantages associated with the use of these glasses. For example, silicate glasses normally melt at very high temperatures, unless they contain significant amount of modifiers, such as alkali metals or alkaline earths metals. Borate glasses, on the other hand, have low temperature melting characteristics, but require substantially high concentrations of alkali metals or alkaline earth metals. Borosilicate glasses can be durable at ambient temperatures and also are melted at temperatures comparable to standard commercial glasses, such as the soda-lime glasses. However, typical commercial borosilicate glasses contain significant amounts of alkali metals, which promote high borate volatility, similar to phosphate glass, during melting. Aluminate glasses exhibit particularly broad emission bandwidths and are attractive for short pulse laser operation. But, these glasses have a very high tendency towards crystallization with a record of being exceptionally difficult to scale up to large scale manufacturing.

Unfortunately, the emission bandwidths achievable in glass hosts are typically many factors smaller than what is possible in the Ti:Sapphire crystal. For high peak power lasers using ultra-short pulses (<100 femto-second pulses or shorter), the emission bandwidths offered by known phosphate laser glasses are too narrow compared to what is needed. In order to overcome this limitation, so-called “mixed” laser glasses are used to achieve the total bandwidth requirement for the petawatt laser system that is in operation and producing the highest peak powers available today. The design of this petawatt laser is shown in, E. Gaul, M. Martinez, J. Blakeney, A. Jochmann, M. Ringuette, D. Hammond, T. Borger, R. Escamilla, S. Douglas, W. Henderson, G. Dyer, A. Erlandson, R. Cross, J. Caird, C. Ebbers, and T. Ditmire, “Demonstration of a 1.1 petawatt laser based on a hybrid optical parametric chirped pulse amplification/mixed Nd:glass amplifier,” Appl. Opt. 49, 1676-1681 (2010). The laser design is shown in FIG. 1 whereas FIG. 2. shows the bandwidth achieved by using the glasses with shifted peak wavelengths. In this mixed laser glass design, phosphate and silicate glasses are used in series to achieve the total bandwidth required for current petawatt laser systems.

However, the present mixed laser glass designs are still insufficient for compact petawatt and for the future exawatt systems capable of producing high energies and short pulses. Mixed glass amplifiers with large enough apertures are expected to be one path forward for generating very high peak powers (100-1000 petawatt) and very short pulses (50-100 fs) in the future.

Thus, mixed glass amplifiers are expected to be one technology used in the future for high peak power, short pulse, multi-petawatt and exawatt laser systems. In these systems, the two glasses, each doped with lasing ions, preferably Nd³⁺ ions, will be used in series. However, the two glasses will have to provide vastly different peak emission wavelengths in order to be viable for the technology to be feasible. One of the glasses in the series will need the shortest possible emission peak for the lasing ion, such as Nd³⁺, while the other one will need the longest possible emission peak for the same lasing ion. All other properties should be optimized for the best laser performance. In general, in mixed glass amplifiers an Nd-doped phosphate glass is used for the shorter emission peak, and an Nd-doped silicate or aluminate glass is used for the higher emission peak.

Most commercially available, large aperture, platinum free, Nd-doped phosphate laser glasses have a peak wavelength of around 1054 nm. The shortest peak wavelength available today for a commercially available, large aperture, platinum free, Nd-doped phosphate glass is 1052.7 nm. On the other hand, the longest commercially available peak wavelength in a glass is 1059.7 nm and it is a Nd-doped silicate glass. To applicants' knowledge, no Nd-doped aluminate laser glasses are commercially available today.

Thus, for high power, short pulse, laser systems, the need exists for large aperture manufacturable rare earth-doped (preferably Nd-doped) laser glasses having peak emission wavelengths that are longer than 1059.7 and shorter than 1052.7 nm.

There are glasses in the literature that show peak wavelengths that are shorter and longer than the peaks mentioned above. Most are silicate glasses with large additions of Ti or Ta. Both of these elements lead to objectionably large non-linear refractive index, but they are needed to obtain the desired peak wavelength and/or bandwidth. L-65, the only previously known aluminate glass for laser applications, contains 52% CaO, 32% A₁₂O₃, 5% BaO and 10.5% SiO₂ with 0.5% Nd₂O₃ doping. Its peak is 1067 nm. However, this glass is not stable enough and has a melting point which is too high for high-homogeneity, Pt-free, large scale manufacture.

Many laser glasses are described in the handbook S. E. Stokowski et al., Nd-doped Laser Glass Spectroscopic and Physical Properties, Lawrence Livermore National Laboratory, University of California, 1981. Of the glasses described therein, the glass having the longest peak wavelength is a glass called 9016, which is a fused silica (CVD grown SiO₂) glass doped with 0.48 wt % Nd₂O₃. This glass has a peak wavelength at 1088 nm. However, the laser properties of glass 9016 are poor, for example, it has a small emission cross section of about 1.4×10⁻²⁰ cm².

In terms of melt properties, in order for the glass to be manufactured on a large scale basis, it is desirable for the glass to have a glass transition temperature T_(g) of less than 850° C. With regards to laser properties, in order for the glass to be commercially useable, the glass preferably has an emission cross section of ≧1.5×10⁻²⁰ cm², and preferably has a nonlinear index, n₂, of <4.0.

In addition, for high power, short pulse, laser systems, the need exists for large aperture manufacturable rare earth-doped (preferably Nd-doped) laser glasses that exhibit a broad emission bandwidth and/or a high emission cross section while also achieving a peak emission wavelength of at least 1059.7 nm, preferably longer than 1059.7.

One aspect of the present invention is to provide a Nd-doped, aluminate-based or silicate-based, laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, 1062 nm or longer, preferably at least 1065 nm nm longer, especially at least 1068 nm or longer, while preferably maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g), high emission cross section, and low nonlinear index, n₂.

Another aspect of the present invention is to provide a Nd-doped acuminate-based laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, 1062 nm or longer, preferably at least 1065 nm nm longer, especially at least 1068 nm or longer, while preferably maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g), high emission cross section, and low nonlinear index, n₂.

Another aspect of the present invention is to provide a Nd-doped silicate-based laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, 1062 nm or longer, preferably at least 1065 nm nm longer, especially at least 1068 nm or longer, while preferably maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g), high emission cross section, and low nonlinear index, n₂.

A further aspect of the present invention is to provide a Nd-doped, aluminate-based or silicate-based, laser glass having an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², for example, 1.6×10⁻²⁰ cm² or higher, preferably at least 1.8×10⁻²⁰ cm² or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

A further aspect of the present invention is to provide a Nd-doped aluminate-based laser glass having an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², for example, 1.6×10⁻²⁰ cm² or higher, preferably at least 1.8×10⁻²⁰ cm² or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

A further aspect of the present invention is to provide a Nd-doped silicate-based, laser glass having an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², for example, 1.6×10⁻²⁰ cm² or higher, preferably at least 1.8×10⁻²⁰ cm² or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

Another aspect of the present invention is to provide a Nd-doped, aluminate-based or silicate based, laser glass having an emission bandwidth (Δλ_(eff)) of ≧28 nm, for example, 30 nm or higher, preferably at least 35 nm or higher, especially at least 40 nm or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

Another aspect of the present invention is to provide a Nd-doped aluminate-based laser glass having an emission bandwidth (Δλ_(eff)) of ≧28 nm, for example, 30 nm or higher, preferably at least 35 nm or higher, especially at least 40 nm or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

Another aspect of the present invention is to provide a Nd-doped silicate based laser glass having an emission bandwidth (Δλ_(eff)) of ≧28 nm, for example, 30 nm or higher, preferably at least 35 nm or higher, especially at least 40 nm or higher, while preferably also achieving a peak emission wavelength of longer than 1059.7 nm and while maintaining properties that render the glass suitable for commercial use, such as low glass transition temperature T_(g) and low nonlinear index, n₂.

According to another aspect of the invention, there is provided a laser system using a mixed-glass arrangement and phase compensation, wherein one of the glasses of the mixed glass system is a Nd-doped, aluminate-based or silicate-based, laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, at least 2 nm longer, preferably at least 5 nm longer, especially at least 8 nm or longer.

According to another aspect of the invention, there is provided a laser system using a mixed-glass arrangement and phase compensation, wherein one of the glasses of the mixed glass system is an Nd-doped silicate-based, laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, 1062 nm or longer.

According to another aspect of the invention, there is provided a laser system using a mixed-glass arrangement and phase compensation, wherein one of the glasses of the mixed glass system is a Nd-doped, aluminate-based or silicate-based, laser glass having an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm² , for example, 1.6×10⁻²⁰ cm² or higher, preferably at least 1.8×10⁻²⁰ cm² or higher, and a peak emission wavelength that is longer than 1059.7 nm.

According to another aspect of the invention, there is provided a laser system using a mixed-glass arrangement and phase compensation, wherein one of the glasses of the mixed glass system is a Nd-doped, aluminate-based or silicate-based, laser glass having an emission bandwidth (Δλ_(eff)) of ≧28 nm, for example, 30 nm or higher, preferably at least 35 nm or higher, especially at least 40 nm or higher, and a peak emission wavelength that is longer than 1059.7 nm.

According to another aspect of the invention, there is provided a laser system wherein the power output of system is at least a pettawatt per pulse or greater, and wherein the system uses a mixed-glass arrangement and phase compensation and one of the glasses of the mixed glass system is a Nd-doped, aluminate-based or silicate-based, laser glass having a peak emission wavelength that is longer than 1059.7 nm, for example, at least 2 nm longer, preferably at least 5 nm longer, especially at least 8 nm or longer.

According to another aspect of the invention, a method is provided for increasing the peak emission wavelength of a Nd-doped, aluminate-based or silicate-based, laser glass by at least 2 nm, preferably at least 5 nm, especially at least 8 nm. For example, the method increases the peak emission wavelength of a Nd-doped laser glass from an average wavelength of about 1060 nm to a wavelength that is greater than about 1060 nm, such as 1062 nm or greater, preferably 1065 nm or greater, especially 1068 nm or greater.

According to a further aspect of the invention, the above-mentioned aluminate-based glass further contains ZnO and/or B₂O₃, for example, by partially substituting ZnO and/or B₂O₃ in place of Al₂O₃. This substitution results in lowering the melt temperature of the aluminate-based glass, which greatly facilitates the ability to scale up the manufacturing process for large scale manufacturing.

According to a further aspect of the invention, the above-mentioned aluminate-based glass further contains Y₂O₃. The yttrium oxide acts to not only reduce the devitirification tendency of the aluminate-based glass, but also facilitates shifting the peak emission wavelength to a higher wavelength.

Also, as described in U.S. Pat. No. 5,526,369, in state-of-the-art high energy laser system designs, a variant of the glass composition employed as the active laser medium can be used as a cladding glass which is attached with adhesives to the edges of slabs or discs fabricated from the active laser glass. The cladding glass composition is generally the same as the lasing glass, except that the lasing species is omitted form the glass (see, for example, the undoped laser fiber cladding glasses described in U.S. Pat. No. 4,217,382). In addition, the lasing species can be omitted and instead the glass is doped with one or more metal species, e.g., Cu or Sm, which impart light-filtering characteristics to the glass for use as doped laser glass claddings. Thus, another aspect of the invention is a cladding glass which has the same composition as the laser glass, except that the lasing ions are omitted and is optionally doped with copper and/or samarium oxides.

Upon further study of the specification and appended claims, further aspects and advantages of this invention will become apparent to those skilled in the art.

These aspects are achieved by incorporating certain metal oxides into the aluminate-based or silicate-based glass host system to achieve a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, while maintaining other laser properties and physical properties that render the glass suitable for commercial use.

In accordance with an embodiment of the invention, there is provided a Nd-doped aluminate glass composition in which the base glass composition comprises (based on mol %):

Al₂O₃ 10.00-45.00 CaO 20.00-65.00 BaO  0.0-15.0 SiO₂  0.0-25.00 B₂O₃  0.0-40.00 Nd₂O₃  0.25-4.00, wherein

the base glass has a molar ratio of CaO to Al₂O₃ of 1.5 to 2.5, and a molar ratio of MO/R₂O₃ in the range of 0.5 to 3.0 (in which, in this case, MO is the sum of BaO+Ca° and R₂O₃ is the sum of Al₂O₃+B₂O₃),

the base glass is modified to contain an amount of Ga₂O₃, ZrO₂, Y₂O₃, Nb₂O₅, Ta₂O₅, Bi₂O₃, and/or ZnO, to achieve a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm,

and wherein the resultant glass has a glass transition temperature T_(g) of less than 850°, and a nonlinear index, n₂, of <4.0.

In general, the base glass is modified to replace part of the proportion of CaO and/or Al₂O₃ with Ga₂O₃, ZrO₂, Y₂O₃, Nb₂O₅, B₂O₃, and/or ZnO. With regards to the individual metal oxides, the resultant glass composition can contain 0.00-40.00 mol % Ga₂O₃, 0.00-10.00 mol % ZrO₂, 0.00-10.00 mol % Y₂O₃, 0.00-10.00 mol % Nb₂O₅, 0.00-20.00 mol % B₂O₃, and/or 0.00-10.00 mol % ZnO. Furthermore, the glass contains at least 5.0 mol % Ga₂O₃, 1.0 mol % ZrO₂, 0.05 mol % Y₂O₃, 1.0 mol % Nb₂O₅, 1.0 mol % B₂O₃, or 0.5 mol % ZnO, and the sum of Al₂O₃, Ga₂O₃, ZrO₂, Y₂O₃, Nb₂O₅, B₂O₃, and ZnO is not more than 40 mol %.

Thus, in accordance with an embodiment of the invention, there is provided a Nd-doped aluminate glass composition comprising (based on mol %):

Al₂O₃  0.00-40.00 CaO 20.00-65.00 BaO  0.0-8.00 SiO₂  0.0-21.00 B₂O₃  0.0-40.00 Nd₂O₃ 0.25-4.00 Ga₂O₃  0.00-40.00 ZrO₂  0.00-10.00 Y₂O₃  0.00-10.00 Nb₂O₅  0.00-10.00 Bi₂O₃  0.00-10.00 ZnO  0.00-10.00 wherein

the glass contains at least 5.0 mol % Ga₂O₃, 1.0 mol % ZrO₂, 0.05 mol % Y₂O₃, 1.0 mol % Nb₂O₅, 0.5 mol % Bi₂O₃, or 0.5 mol % ZnO,

the sum of Al₂O₃, Ga₂O₃, ZrO₂, Y₂O₃, Nb₂O₅, B₂O₃, Bi₂O₃, and ZnO is not more than 60 mol %,

the glass composition exhibits a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and

the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.

In addition, the Nd-doped aluminate glass composition according to the invention may further contain 0.0-10 mol % of R′₂O₃, wherein R′₂O₃ is the sum of Gd₂O₃ and La₂O₃,

Further, the Nd-doped aluminate glass composition according to the invention may contain 0.0-10.00 mol % of M₂O, wherein M₂O is the sum of Li₂O, Na₂O, K₂O, and Cs₂O.

Further, the Nd-doped aluminate glass composition according to the invention may contain 0.0-10.00 mol % of M′O, wherein M′O is the sum of MgO, CaO, and SrO.

In accordance with another embodiment of the invention, the Nd-doped aluminate glass composition comprises (based on mol %):

Al₂O₃ 15.00-40.00 CaO   45-62.00 BaO 0.0-5.0 SiO₂  5.00-10.00 Nd₂O₃ 0.25-3.00 Ga₂O₃  0.00-35.00 ZrO₂ 0.00-8.00 Y₂O₃ 0.00-8.00 Nb₂O₅ 0.00-8.00 B₂O₃  0.00-10.00 ZnO  0.00-10.00 R₂O₃ 0.00-5.00 M₂O 0.00-5.00 M′O 0.00-5.00 wherein

the glass contains at least 5.0 mol % Ga₂O₃, 1.0 mol % ZrO₂, 0.05 mol % Y₂O₃, 1.0 mol % Nb₂O₅, 0.5 mol % Bi₂O₃, or 0.5 mol % ZnO, and

the sum of Al₂O₃, Ga₂O₃, ZrO₂, Y₂O₃, Nb₂O₅, Bi₂O₃, and ZnO is not more than 40 mol %.

R₂O₃ is the sum of Gd₂O₃ and La₂O₃,

M₂O is the sum of Li₂O, Na₂O, K₂O, and Cs₂O,

M′O is the sum of MgO, CaO, and SrO, the glass composition exhibits a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and

a glass transition temperature T_(g) of less than 850° C., and

a nonlinear index, n₂, of <4.0.

In accordance with another embodiment of the invention, there is provided a Nd-doped sodium-silicate glass composition in which the base glass composition comprises (based on mol %):

SiO₂ 40.00-75.00 Na₂O 10.00-35.00 B₂O₃  0.00-20.00 Nd₂O₃ 0.25-4.00 Sb₂O₃ 0.00-1.00 wherein the sum of the amounts of SO₂ and Na₂O in the base glass is at least 84.5 mol %; and

wherein the base class is modified to contain an amount of ZrO₂, Nb₂O₅, Ta₂O₅, Y₂O₃, and/or La₂O₃, to achieve a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and

the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.

In general, the base glass is modified to replace part of the proportion of SiO₂ and/or Na₂O with ZrO₂, Nb₂O₅, Ta₂O₅, Y₂O₃, and/or La₂O₃. With regards to the individual metal oxides, the resultant glass composition can contain 0.00-20.00 mol % ZrO₂, 0.00-20.00 mol % Nb₂O₅, 0.00-15.00 mol % Ta₂O₅, 0.00-20.00 mol % Y₂O₃, and/or 0.00-20.00 mol % La₂O₃. Furthermore, the glass contains at least 1.0 mol % ZrO₂, 1.0 mol % Nb₂O₅, 0.5 mol % Ta₂O₅, 0.05 mol % Y₂O₃, or 0.5 mol % La₂O₃.

Thus, in accordance with an embodiment of the invention, there is provided a Nd-doped sodium-silicate glass composition comprising (based on mol %):

SiO₂ 40.00-75.00 Na₂O 10.00-35.00 B₂O₃  0.00-20.00 Nd₂O₃ 0.25-4.00 Sb₂O₃ 0.00-1.00 ZrO₂  0.00-20.00 Nb₂O₅  0.00-20.00 Ta₂O₅  0.00-15.00 Y₂O₃  0.00-20.00 La₂O₃  0.00-20.00 wherein

the glass contains at least 1.0 mol % ZrO₂, 1.0 mol % Nb₂O₅, 0.5 mol % Ta₃O₅, 0.05 mol % Y₂O₃, or 0.5 mol % La₂O₃,

the glass a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and

the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.

In accordance with another embodiment of the invention, the Nd-doped sodium-silicate glass composition comprises (based on mol %):

SiO₂ 50.00-72.00 Na₂O 10.00-22.00 B₂O₃  4.00-20.00 Nd₂O₃ 0.25-5.00 Sb₂O₃ 0.05-1.00 wherein

wherein the glass contains at least 1.0 mol % ZrO₂, 1.0 mol % Nb₂O₅, 0.5 mol % Ta₂O₅, 0.05 mol % Y₂O₃, or 0.5 mol % La₂O₃,

the glass a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.

With regards to ranges described herein, all ranges include at least the two endpoints of the ranges, as well as all units between the two endpoints. Thus, for example, a range of 1 to 10 is to be understood as expressly disclosing at least the values of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10.

In the aluminate base glass, Al₂O₃ functions as the primary network former. Thus, according to another aspect, the aluminate glass composition according to the invention contains 0.00-40.00 mol % of Al₂O₃, for example, 10.00-40.00 mol % of Al₂O₃, e.g., 20.00-40.00 mol % Al₂O₃, or 27.00-40.00 mol % Al₂O₃, or 27.00-35.00 mol % Al₂O₃, or 27.00-32,00 mol % Al₂O₃.

In the aluminate glass composition, CaO in general functions as an intermediate glass former working in conjunction with Al₂O₃ to form the glass, Thus, according to another aspect, the aluminate glass composition according to the invention contains 20.00-65.00 mol % of Ca° , for example, 30.00-60.00 mol % of CaO, or 35.00-55.00 mol % Ca° , or 40.00-55.00 mol % CaO, or 45.00-55.00 mol % CaO.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-8.00 mol % of BaO, for example, 2.00-8.00 mol % BaO, or 3.00-7.00 mol % BaO, or 4.00-6.00 mol % BaO. In this glass composition, BaO also generally acts as a glass modifier.

In the aluminate glass composition, SiO₂ generally acts as a network co-former. Thus, according to another aspect, the aluminate glass composition according to the invention contains 0.00-21.00 mol % of SiO₂, for example, 5.00-20.00 mol % of SiO₂, or 5.00-15.00 mol % SiO₂, or 8.00-15.00 mol % SiO₂, or 8.00-12.00 mol % SiO₂.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-40.00 mol % of B₂O₃, for example, 1.00-40.00 mol % of B₂O₃, or 0.00-35.00 mol % of B₂O₃, or 0.00-30.00 mol % of B₂O₃, or 0.00-25.00 mol % of B₂O₃, or 1,00-20.00 mol % of B₂O₃, or 0.00-15.00 mol % of B₂O₃, or 0.00-10.00 mol % of B₂O₃, or 0.00-8.00 mol % of B₂O₃, or 2.00-8.00 mol % of B₂O₃, or 3.00-7.00 mol % of B₂O₃.

Nd₂O₃ provides the lasing ions for the glass composition. According to another aspect of the invention, the aluminate glass composition according to the invention contains 0.25-4.00 mol % of Nd₂O₃, for example, 0.25-3.00 mol % Nd₂O₃, or 0.25-2.00 mol % Nd₂O₃, or 0.25-1.00 mol % Nd₂O₃.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-40.00 mol % of Ga₂O₃, for example, 5.00-40.00 mol % of Ga₂O₃, or 0.00-35.00 mol % of Ga₂O₃, or 5.00-35.00 mol % of Ga₂O₃, or 10.00-35.00 mol % of Ga₂O₃.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-10.00 mol % of ZrO₂, for example, 1.00-10.00 mol % of ZrO₂, or 0.00-8.00 mol % of ZrO₂, or 2.00-8.00 mol % of ZrO₂ or 3.00-7.00 mol % of ZrO₂.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-10.00 mol % of Y₂O₃, for example, 0.05-10.00 mol % of Y₂O₃, or 0.00-8.00 mol % of Y₂O₃, or 2.00-8.00 mol % of Y₂O₃, or 2.00-7.00 mol % of Y₂O₃.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-10.00 mol % of Nb₂O₅, for example, 1.00-10.00 mol % of Nb₂O₅, or 0.00-8.00 mol % of Nb₂O₅, or 2.00-8.00 mol % of Nb2O₅, or 3.00-7.00 mol % of Nb₂O₅.

According to another aspect, the aluminate glass composition according to the invention contains 0.50-10.00 mol % of Bi₂O₃, for example, 0.75-8.00 mol % of Bi₂O₃, or 0.75-7.00 mol % of Bi₂O₃, or 0.75-6.00 mol % of Bi₂O₃, or 0.75-5.00 mol % of Bi₂O₃.

According to another aspect, the aluminate glass composition according to the invention contains 0.00-10.00 mol % of ZnO, for example, 0.50-10.00 mol % of ZnO, or 1.00-10.00 mol % of ZnO, or 3.00-10.00 mol % of ZnO, or 5.00-10.00 mol % of ZnO.

According to another aspect, the sodium-silicate glass composition according to the invention contains, for example, 40.00-72.00 mol % of SiO₂, for example, 40.00-70.00 mol % of SiO₂, or 45.00-65.00 mol % of SiO₂ or 45.00-60.00 mol % of SiO₂, or 50.00-60.00 mol % of SiO₂.

According to another aspect, the sodium-silicate glass composition according to the invention contains 10.00-35.00 mol % of Na₂O, for example, 15.00-35.00 mol % of Na₂O, or 15.00-25.00 mol % of Na₂O, or 16.00-25.00 mol % of Na₂O or 18.00-25.00 mol % of Na₂O, or 18.00-23.00 mol % of Na₂O.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-20.00 mol % of B₂O₃, for example, 1.00-18.00 mol % of B₂O₃, or 5.00-18.00 mol % of B₂O₃, or 5.00-15.00 mol % of B₂O₃, or 10.00-18.00 mol % of B₂O₃.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.25-4.00 mol % of Nd₂O₃, for example, 1.00-4.00 mol % of Nd₂O₃ or 1.00-2.50 mol % of Nd₂O₃.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-20.00 mol % of ZrO₂, for example, 1.00-20.00 mol % of ZrO₂, or 0.00-15.00 mol % of ZrO₂, or 0.00-10,00 mol % of ZrO₂, or 0.00-8.00 mol % of ZrO₂, or 1.00-8.00 mol % of ZrO₂, or 2.00-8.00 mol % of ZrO₂, or 3.00-7.00 mol % of ZrO₂.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-20.00 mol % of Nb₂O₅, for example, 1.00-20.00 mol % of Nb₂O₅, or 0.00-15.00 mol % of Nb₂O₅, or 0.00-10.00 mol % of Nb₂O₅, or 0.00-8.00 mol % of Nb₂O₅, or 1.00-8.00 mol % of Nb₂O₅, or 2.00-8.00 mol % of Nb₂O₅, or 3.00-7.00 mol % of Nb₂O₅.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-15.00 mol % of Ta₂O₅, for example, 0.50-15.00 mol % of Ta₂O₅, or 0.00-12.00 mol % of Ta₂O₅, or 0.00-10.00 mol % of Ta₂O₅, or 0.00-8.00 mol % of Ta₂O₅, or 1.00-8.00 mol % of Ta₂O₅, or 2.00-8.00 mol % of Ta₂O₅, or 3.00-7.00 mol % of Ta₂O₅.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-20.00 mol % of Y₂O₃, for example, 0.50-20.00 mol % of Y₂O₃, or 1.00-20.00 mol % of Y₂O₃, or 0.00-15.00 mol % of Y₂O₃, or 0.00-10.00 mol % of Y₂O₃, or 0.00-8.00 mol % of Y₂O₃, or 0.50-8.00 mol % of Y₂O₃, or 2.00-8.00 mol % of Y₂O₃, or 3.00-7.00 mol % of Y₂O₃.

According to another aspect, the sodium-silicate glass composition according to the invention contains 0.00-20.00 mol % of La₂O₃, for example, 0.50-20.00 mol % of La₂O₃, or 1.00-20.00 mol % of La₂O₃, or 0.00-15.00 mol % of La₂O₃, or 0.00-10.00 mol % of La₂O₃, or 0.00-8.00 mol % of La₂O₃, or 0.50-8.00 mol % of La₂O₃, or 2.00-8.00 mol % of La₂O₃, or 3.00-7.00 mol % of La₂O₃.

With regards to the additional components, the glass contains a maximum of 4 weight percent, especially a maximum of 2 weight percent, of conventional additives or impurities, such as refining agents (e.g., As₂O₃ and Sb₂O₃) and antisolarants (e.g., Nb₂O₅). In addition, the glass composition may contain halides to help dry the melt or residual water and to help refining of the glass. For example, the glass composition may contain up to 9 wt % F, preferably not more 5 wt %, and, up to 5wt % Cl, although Cl is less preferred than F.

In accordance with another aspect of the invention, the aluminate or sodiumsilicate glass compositions according to the invention possesses a peak emission bandwidth of at least 1060 nm, preferably at least 1061m, especially at least 1065 nm, for example 1060 nm-1069 nm or 1060nm-1068 nm or 1060 nm-1067 nm.

In accordance with another aspect of the invention, the aluminate or sodium silicate glass compositions according to the invention possesses an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², preferably at least 1.8×10⁻²⁰ cm, especially at least 2.0×10⁻²⁰ cm, for example 1.6×10⁻²⁰-2.8×10⁻²⁰ cm or 1.8×10⁻²⁰-2.7×10⁻²⁰ or 2.0×10⁻²⁰-2.7×10⁻²⁰.

In accordance with another aspect of the invention, the aluminate or sodium silicate glass compositions according to the invention possesses an effective emission bandwidth (Δλ_(eff)) of at least 30 nm, preferably at least 35 nm, especially at least 37 nm, and in particular at least 40 nm, for example 34-40 nm or 38-40 nm.

Laser properties can be measured in accordance with the Judd-Ofelt theory, the Fuchtbauer-Ladenburg theory, or the McCumber method. A discussion of the Judd-Ofelt theory and the Fuchtbauer-Ladenburg theory can be found in E. Desurvire, Erbium Doped Fiber Amplifiers, John Wiley and Sons (1994). The McCumber method is as discussed in, for example, Miniscalco and Quimby, Optics Letters 16 (4) pp 258-266 (1991). See also Kassab, Journal of Non-Crystalline Solids 348 (2004) 103-107. The Judd-Ofelt theory and the Fuchtbauer-Ladenburg theory evaluate laser properties from an emission curve, whereas the McCumber method uses the absorption curve of the glass.

Regarding emission bandwidth, if one has a measured emission curve (such as collected in a Judd-Ofelt or Fuchtbauer-Ladenburg analysis) or a calculated emission curve (from a McCumber analysis) one can get emission bandwidth in two ways. The first way is to simply measure the width at half of the maximum value (called emission bandwidth full width half maximum or Δλ_(FWHM)).

The second method divides every point on the emission curve by the total area under the curve. The result, called a linewidth function, will have a peak value that is defined as the inverse of the effective bandwidth, Δλ_(eff). By this method the entire emission curve always contributed to the emission bandwidth result. It is this value used herein in the analysis as the best indicator of emission bandwidth.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention and further details, such as features and attendant advantages, of the invention are explained in more detail below on the basis of the exemplary embodiments which are diagrammatically depicted in the drawings, and wherein:

FIG. 1 graphically illustrates the shift in the peak emission wavelength of an aluminate base glass to a longer wavelength and broadening of the emission cross section due to the addition of ZnO; and

FIG. 2 graphically illustrates the shift in the peak emission wavelength of an sodium-silicate base glass to longer wavelengths and the broadening of the emission cross section due to the addition of B₂O₃ and transition metal oxides.

EXAMPLES

All of the glasses were made using laser grade ingredients and melted under a dry oxygen environment with the help of stirring using a platinum stirrer for better homogeneity. All of the glasses were cast into a mold and this was appropriately annealed in order to remove the stress as the liquid cools to the amorphous state. The resulting glass slab was shaped into forms required for use with the instruments that provide various properties for

Tables 1A-1C list aluminate compositions in accordance with the invention, and Table 3 lists sodium-silicate compositions in accordance with the invention. The results of these property measurements and calculations are detailed in Tables 2A-2C for the aluminate glasses according to the invention and in Table 4 for the sodium-silicate glasses according to the invention.

TABLE 1A Aluminate Based Glass System Metal Oxide Base (mol %) Glass Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 CaO 52.00 52.00 52.00 52.00 52.00 47.00 47.00 47.00 Nd₂O₃ 0.50 0.50 0.50 0.50 0.50 0.50 0.50 0.50 BaO 5.00 5.00 5.00 5.00 5.00 5.00 5.00 5.00 SiO₂ 10.50 10.50 10.50 10.50 10.50 10.50 10.50 10.50 Al₂O₃ 32.00 20.00 27.00 27.00 32.00 32.00 32.00 Ga₂O₃ 12.00 32.00 ZrO₂ 5.00 Y₂O₃ 5.00 MoO₂ 5.00 WO₃ 5.00 Ta₂O₅ 5.00

TABLE 1B Aluminate Based Glass System Metal Oxide Base (mol %) Glass Ex. 8 Ex. 9 Ex. 10 Ex. 11 Ex. 12 Ex. 13 Ex. 14 CaO 52.00 47.00 49.50 47.00 52.00 52.00 52.00 52.00 Nd₂O₃ 0.50 0.50 0.50 0.50 0.50 0.50 0.50 0.50 BaO 5.00 5.00 4.70 5.00 5.00 5.00 5.00 5.00 SiO₂ 10.50 10.50 10.00 10.50 10.50 10.50 10.50 10.50 Al₂O₃ 32.00 32.00 19.00 27.00 22.70 22.00 30.75 Ga₂O₃ 11.40 32.00 ZrO₂ 4.80 5.00 Nb₂O₅ 5.00 B₂O₃ 5.00 ZnO 9.30 7.50 Y₂O₃ 2.50 La₂O₃ 1.25

TABLE 1C Aluminate Based Glass System Metal Oxide Base (mol %) Glass Ex. 15 Ex. 16 Ex. 17 Ex. 18 Ex. 19 Ex. 20 Ex. 21 CaO 52.00 52.00 52.00 52.00 52.00 47.00 47.00 47.00 Nd₂O₃ 0.50 0.50 0.50 0.50 0.50 0.50 0.50 0.50 BaO 5.00 5.00 5.00 5.00 5.00 5.00 5.00 5.00 SiO₂ 10.50 10.50 10.50 10.50 10.50 10.50 10.50 10.50 Al₂O₃ 32.00 27.00 31.00 31.12 30.88 32.00 32.00 27.00 TiO₂ 5.00 B₂O₃ 5.00 Ta₂O₅ 1.00 Bi₂O₃ 0.88 Gd₂O₃ 1.12 Na₂O 5.00 Li₂O 5.00 SrO 5.00

TABLE 2A Laser Properties of Aluminate Based Glasses Laser Base Properties Glass Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 λ_(Peak) [nm] 1067.00 1067.02 High 1068.12 1068.80 High High High Δλ_(eff) [nm] 48.26 45.47 temperature 46.11 47.15 temperature temperature temperature Peak σ_(em) 1.8 1.9 melting 2.5 2.3 melting melting melting [10⁻²⁰ cm²] Δλ_(FWHM) [nm] 41.2 37.3 37.5 38.6 τ_(R) [μsec] 349 348 262 261 Ω₂ [10⁻²⁰ cm²] 4.9 5.2 5.1 4.7 Ω₄ [10⁻²⁰ cm²] 4.2 3.3 4.4 5.6 Ω₆ [10⁻²⁰ cm²] 4.0 4.4 5.8 4.7 Non-linear 2.92 3.34 3.11 3.13 index, n₂ Glass Transition >835.00 799.5 820.3 826.5 Temp. T_(g)

TABLE 2B Laser Properties of Aluminate Based Glasses Laser Base Properties Glass Ex. 8 Ex. 9 Ex. 10 Ex. 11 Ex. 12 Ex. 13 Ex. 14 λ_(Peak) [nm] 1067.00 1065.89 1067.10 1065.87 1065.64 1067.74 1068.75 Crystals Δλ_(eff) [nm] 48.26 42.12 43.50 42.11 43.39 46.81 47.47 in bulk Peak σ_(em) 1.8 2.2 2.6 2.5 2.3 2.0 1.9 [10⁻²⁰ cm²] Δλ_(FWHM) [nm] 41.2 29.8 36.1 34.8 35.4 37.6 39.1 τ_(R) [μsec] 349 287 267 253 309 324 304 Ω₂ [10⁻²⁰ cm²] 4.9 6.3 4.7 4.2 4.1 4.9 4.3 Ω₄ [10⁻²⁰ cm²] 4.2 4.1 4.1 4.8 4.4 4.0 4.6 Ω₆ [10⁻²⁰ cm²] 4.0 4.1 5.6 4.4 4.7 4.3 4.1 Non-linear 2.92 NA* 3.64 5.27 2.52 3.29 3.35 index, n₂ Glass Transition >835.00 801.3 816.3 759.0 774.5 740.2 749.6 Temp. T_(g) *NA = not available

TABLE 2C Laser Properties of Aluminate Based Glasses Laser Base Properties Glass Ex. 15 Ex. 16 Ex. 17 Ex. 18 Ex. 19 Ex. 20 Ex. 21 λ_(Peak) [nm] 1067.00 Crystals Crystals 1067.94 1067.77 Devitrified 1067.64 1064.00 Δλ_(eff) [nm] 48.26 in bulk in bulk 46.76 NA NA NA Peak σ_(em) 1.8 1.9 2.0 2.01 2.3 [10⁻²⁰ cm²] Δλ_(FWHM) [nm] 41.2 37.6 NA NA NA τ_(R) [μsec] 349 324 316.8 337.6 304 Ω₂ [10⁻²⁰ cm²] 4.9 4.8 4.5 4.37 3.76 Ω₄ [10⁻²⁰ cm²] 4.2 4.3 4.6 4.13 4.66 Ω₆ [10⁻²⁰ cm²] 4.0 4.3 4.3 4.1 4.83 Non-linear 2.92 3.06 NA 2.82 2.46 index, n₂ Glass Transition >835.00 817.5 825.2 802 NA Temp. T_(g) * NA = not available

TABLE 3 Sodium Silicate Based Glass System Base Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Glass 22 23 24 25 26 27 28 29 Oxide Mol % SiO₂ 66.60 73.00 60.00 60.00 60.00 57.00 57.00 57.00 60.00 Al₂O₃ 3.00 3.00 3.00 B₂O₃ 5.00 15.00 15.00 15.00 15.00 15.00 15.00 15.00 Na₂O 33.30 22.00 20.00 20.00 20.00 20.00 20.00 20.00 20.00 ZrO₂ 5.00 5.00 Nb₂O₅ 5.00 Ta₂O₅ 5.00 5.00 Y₂O₃ 5.00 La₂O₃ 5.00 Nd₂O₃ 0.63 0.63 0.63 0.63 0.63 0.63 0.63 0.63 0.63 Sb₂O₃ 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10

TABLE 4 Laser Properties of Sodium Silicate Based Glasses Property Base Glass Ex. 22 Ex. 23 Ex. 24 Ex. 25 Ex. 26 Ex. 27 Ex. 28 Ex. 29 λ_(Peak calibrated) [nm] 1059.18 1059.18 1061.40 1060.46 1060.92 1060.48 1059.97 1061.01 1061.00 Δλ_(eff) [nm] 33.60 35.65 39.25 38.88 40.14 40.98 39.35 36.84 NA Peak σ_(em) [10⁻²⁰ cm²] 1.83 1.57 1.64 2.06 1.88 1.9 2.2 2.6 2.43 Δλ_(FWHM) [nm] 25.30 27.30 29.40 31.40 31.00 31.8 31.0 29.2 NA τ_(R) [μsec] 573.60 626.40 521.30 401.00 446.70 432 376 355 376 Ω₂ [10⁻²⁰ cm²] 3.81 3.96 4.70 6.80 6.44 5.0 6.5 4.2 4.46 Ω₄ [10⁻²⁰ cm²] 3.29 3.05 3.42 4.16 4.40 4.0 4.3 4.5 4.6 Ω₆ [10⁻²⁰ cm²] 3.30 2.98 3.30 3.99 3.82 4.1 4.3 4.9 4.65 Non-linear 1.41 1.28 1.50 2.27 2.23 1.51 2.14 1.57 1.46 index, n₂ Glass Transition 471.5 525.9 620.3 618.5 643.4 564.0 573.0 557.0 583.0 Temp. T_(g)

As can be seen from Tables 2A-2C, the base aluminate glass example exhibits a long peak emission wavelength of 1067 nm and a broad effective emission bandwidth (Δλ_(eff)) of 48.26 nm, as well as a high emission cross section (σ_(em)) of 1.8×10⁻²⁰ cm². However, this glass exhibits a very high glass transition temperature, T_(g), of >835° C., thereby rendering the glass unsuitable for commercialization.

In Example 1, replacing part of the Al₂O₃ of the base aluminate glass with Ga₂O₃, broadens the peak emission bandwidth without adversely impacting the peak emission wavelength. In addition, the glass of Example 1 has a higher emission cross section (σ_(em)) of 1.9×10⁻²⁰ cm². Although the effective emission bandwidth (Δλ_(eff)) for Example 1 is lower (i.e., 45.47 nm), the emission bandwidth is still very large.

In Examples 3-4, replacing part of the Al₂O₃ of the base aluminate glass with the transition metals ZrO₂ and Y₂O₃, appreciably increased the emission cross section (σ_(em)) (2.5×10⁻²⁰ cm² and 2.5×10⁻²⁰ cm²) while also increasing the length of the peak emission wavelength by 1-2 nm. Here again, while the effective emission bandwidth (Δλ_(eff)) for Examples 3 and 4 are lower than that of the base glass example (i.e., 46.11 nm and 47.15 nm), the emission bandwidth is still quite large.

In Example 8, replacing part of the CaO of the base aluminate glass with the Nb₂O₅, decreased the length of the peak emission wavelength, but still was very long, i.e., 1065.89 nm. Also, while the effective emission bandwidth (Δλ_(eff)) was lower (42.12 nm), the emission cross section (σ_(em)) did appreciably increase (i.e., 2.2×10⁻²⁰ cm²). Similar results were achieved when replacing part of the Al₂O₃with B₂O₃. See Example 11.

Combing Ga₂O₃ with a transition metal, ZrO₂, significantly increases the peak emission cross-section and slightly increases the length of the peak emission wavelength. See Example 9. In Example 10, which combines a higher amount of Ga₂O₃ with a transition metal, ZrO₂, the peak emission cross-section remains high and the length of the peak emission wavelength slightly decreases.

In Example 12, the addition of ZnO results in an appreciable increase in the length of the peak emission wavelength and an appreciable increase the peak emission cross-section. in Example 13, the combination of Y₂O₃ and ZnO results in an even greater increase in the length of the peak emission wavelength. The presence of ZnO also provides the added advantage of lowering the melt temperature of the aluminate-based glass. By lowering of the melt temperature of the aluminate-based glass allows the glass to be melted in a standard electrically heated furnace, which greatly facilitates the ability to scale up of the manufacturing process.

Replacing part of the Al₂O₃ with Bi₂O₃ both increased the peak emission cross-section bandwidth and the peak emission wavelength. See Example 17. Similarly, replacing part of the Al₂O₃ with Gd₂O₃ increased the peak emission cross-section bandwidth and the peak emission wavelength. See Example 18. Replacing part of the CaO with SrO also increased the peak emission wavelength, See Example 20. Replacing part of CaO and Al₂O₃ with B₂O₃ and Li₂O decreased peak emission wavelength, but increased the peak emission cross-section bandwidth.

As can be seen from Example 22, replacing part of the Na₂O of the base sodium silicate glass with B₂O₃ increased the peak emission bandwidth (from 33.60 nm to 35.65 nm) without adversely affecting the peak emission wavelength exhibited by the base silicate glass composition (i.e., 1059.18 nm). On the other hand, when amounts of SiO₂ and Na₂O are replaced by B₂O₃ and ZrO₂, the peak emission wavelength was appreciably increased, while the peak emission bandwidth also increased. See Example 23. Further, replacing amounts of SiO₂ and Na₂O by B₂O₃ and Nb₂O₅ appreciably increased both the peak emission wavelength and the emission bandwidth, and increased the emission cross section (2.06×10⁻²⁰ cm² v. 1.83×10⁻²⁰ cm²). See Example 24. When amounts of SiO₂ and Na₂O are replaced by B₂O₃ and Ta₂O₅, a greater increase in peak emission wavelength and the emission bandwidth are obtained, and the emission cross section also increased. See example 25.

It is important to note that the gains in the emission bandwidth and peak wavelength, did not reduce the emission cross-section in examples 23 and 24. According to Füchtbauer and Ladenburg, this requires a reduction of the radiative lifetime (τ_(R)) which can also be seen to occur in the figure. It is generally desirable to maintain lifetime values greater than ˜200 μs in order to allow efficient pumping by flash lamp, while also maintaining a cross-section of ˜2.0×10⁻²⁰ cm² in order to allow efficient energy storage and extraction. This minimum value for lifetime is exceeded for all examples herein, and the minimum cross-section target is maintained for examples 3, 4, 8-12 and 23, illustrating the particular utility of ZnO, Y₂O₃, Nb₂O₅ and B₂O₃, as these oxides can serve to increase both bandwidth and emission cross-section in both glass systems.

In Examples 26-28 part of the SiO₂ of the base sodium silicate glass is replaced by a combination of Al₂O₃ and ZrO₂, Ta₂O₅ or with La₂O₃. In each case, in comparison to the base sodium silicate glass, the glass exhibited a higher peak emission wavelength, an increased peak emission bandwidth, and an increased emission cross section (2.6×10⁻²⁰ cm² in the case of Example 28). In Example 29, part of the SiO₂ and part of Na₂O are replaced with B₂O₃ and Y₂O₃. This resulted in a higher peak emission wavelength and an increased emission cross section.

The entire disclosure[s] of all applications, patents and publications, cited herein, are incorporated by reference herein.

The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. 

1-16. (canceled)
 17. A Nd-doped sodium-silicate glass composition comprising (based on mol %): SiO₂ 40.00-75.00 Na₂O 10.00-35.00 B₂O₃  0.00-20.00 Nd₂O₃ 0.25-4.00 Sb₂O₃ 0.00-1.00 ZrO₂  0.00-20.00 Nb₂O₅  0.00-20.00 Ta₂O₅  0.00-15.00 Y₂O₃  0.00-20.00 La₂O₃  0.00-20.00

wherein the glass contains at least 1.0 mol % ZrO₂, 1.0 mol % Nb₂O₅, 0.5 mol % Ta₂O₅, 0.05 mol % Y₂O₃, or 0.5 mol % La₂O₃, the glass a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.
 18. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 15.00-35.00 mol % of Na₂O.
 19. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 1.00-18.00 mol % of B₂O₃.
 20. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 1.00-4.00 mol % of Nd₂O₃.
 21. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 1.00-20.00 mol % of ZrO₂.
 22. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 1.00-20.00 mol % of Nb₂O₅.
 23. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 0.50-15.00 mol % of Ta₂O₅.
 24. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 0.50-20.00 mol % of Y₂O₃.
 25. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition contains 0.50-20.00 mol % of La₂O₃.
 26. The Nd-doped sodium-silicate glass composition according to claim 17, wherein said glass composition comprises (based on mol %): SiO₂ 50.00-72.00 Na₂O 10.00-22.00 B₂O₃  4.00-20.00 Nd₂O₃ 0.25-5.00 Sb₂O₃ 0.05-1.00

wherein wherein the glass contains at least 1.0 mol % ZrO₂, 1.0 mol % Nb₂O₅, 0.5 mol % Ta₂O₅, 0.05 mol % Y₂O₃, or 0.5 mol % La₂O₃, the glass a peak emission wavelength of longer than 1059.7 nm, and/or an emission cross section (σ_(em)) of ≧1.5×10⁻²⁰ cm², and/or an emission bandwidth (Δλ_(eff)) of ≧25 nm, and the glass has a glass transition temperature T_(g) of less than 850° C., and a nonlinear index, n₂, of <4.0.
 27. In a solid state, mixed glass, laser system comprising a Nd-doped phosphate glass and another Nd-doped glass as the solid gain medium and a pumping source, the improvement wherein said another Nd-doped glass is a glass having a composition in according to claim
 17. 28. A laser system according to claim 27, wherein the power output of system is at least a pettawatt per pulse or greater.
 29. A method for generating a laser beam pulse comprising flashlamp pumping or diode pumping the solid gain medium of the laser system according to claim
 27. 